- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05721703
An Observational Study of Long-term Peritoneal Dialysis Patients Who Eventually Develop Ultrafiltration Failure (LUFF) (LUFF)
Observe the Multi-indices of Long-term Peritoneal Dialysis Patients to Explore the Evolution of Peritoneal Ultrafiltration Failure
Study Overview
Status
Conditions
Detailed Description
Background: Chronic kidney disease (CKD) is one of the most common non-communicable diseases. The Global Burden of Disease (GBD), which examined multiple diseases in 188 countries from 1990 to 2013, found that the number of CKD patients increased from 318,665,000 to 47,1916,000, representing a 48% increase in prevalence (2.1% annually). Peritoneal dialysis is an important renal replacement therapy for participants with end-stage renal disease. The removal of water mainly depends on the high osmotic pressure of dialysate which is called ultrafiltration, and the loss of ultrafiltration function of peritoneum is called ultrafiltration failure. Data from the National Blood Purification Case Information System (CNRDS) show that the rate of conversion from ultrafiltration failure to hemodialysis is 5%-10%, and cardiovascular complications caused by fluid overload, such as malignant hypertension and heart failure, are the common causes of death. At the end of 2021, dialysis data in mainland China showed that there were nearly 880,000 patients undergoing dialysis treatment, of which 14% chose peritoneal dialysis, the average dialysis age of peritoneal dialysis patients was 50.3 months, the proportion of patients who had been on dialysis for more than 5 years was 33.9%, and the proportion of patients who had been on dialysis for more than 10 years was 7.5%. It can be seen that long-term peritoneal dialysis still has a high shedding rate, and ultrafiltration failure is the key problem of long-term peritoneal dialysis.
Methods: Investigators gathered participants from Department of Nephrology, PLA General Hospital, from May 2021 to May 2029. Inclusion Criteria: 1.Clinically diagnosed as chronic renal insufficiency (CKD 5); 2.Incident PD patients who were newly inserted PD catheter during the observation period of this study; 3.Prevalent PD patients who inserted PD cather before initiation of this study, should be admitted as pre-UFF, has taken long-term PD(>5 years) before removing cather during the observation period of this study; 4.Written informed consent signed by the patient or the authorized client has been obtained. Exclusion Criteria: 1.Acute renal failure; 2.Pregnant or lactating women; 3.Active infection duration; 4.One of infectious serum markers of HIV, syphilis, hepatitis B and hepatitis C is positive; 5.Any other conditions that the investigator considers impossible to join this trial. The observed indices were: (1)Demographic characteristics; (2)Peritoneal equilibration test (PET D/P), adequacy assessment(Ccr, Kt/V), evaluation of ultrafiltration (urine volume, intake,etc.); (3)Peritoneal dialysate routine examination, peritoneal dialysate inflammation examination and other markers and exosome examination; (4)Classification and counting of exfoliated cells from peritoneal dialysis effluent, and dialysate exfoliated cells primary culture for further cell biology analysis; (5)Peritoneal histopathology and immunohistochemical analysis and proteomics and single cell transcriptome analysis; (6)Clinical examinations: Routine blood test, Uroscopy, Blood biochemistry test, Coagulation function test, Immunoassay, Bone metabolism test, Thyroid function test, Evaluation of Ascites, etc. For an incident PD patient,after admission,the peritoneal catheter was inserted, and the data of the initial peritoneal equilibration test and clinical examinations were collected, and the peritoneal membrane was sampled for single-cell analysis. After that, the patient was followed up, and the data of the subsequent peritoneal equilibration test and clinical examinations were collected until the end point(technique failure) or the study end(8 years). The investigators collected the peritoneal tissue for single-cell sequencing when participants remove the catheters(for the technique failure patients). If the catheter is still in use when this study stop collecting data(8 years), the peritoneal dialysis effluent will substitute for peritoneal tissue to the morphological and single-cell analysis. For a prevalent patient who admitted as pre-UFF, investigators collected the final peritoneal equilibration test and clinical examination data then sample the peritoneal tissue for single-cell sequencing when removing the cather. SPSS and R were used for statistical analysis. Continuous variables were expressed as mean ± standard deviation, and discontinuous variables were expressed as percentage. The independent t-test or chi-square test was used for comparison between the two data. P<0.05 was statistically significant.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Beijing
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Beijing, Beijing, China, 100853
- Chinese PLA General Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Clinically diagnosed as chronic renal insufficiency (CKD 5)
- Patients who met the first dialysis guidelines for peritoneal dialysis without catheter, or patients with peritoneal dialysis regularly, or ultrafiltration failure was diagnosed and patients on peritoneal dialysis were to be existed.
- Written informed consent signed by the patient or the authorized client has been obtained.
Exclusion Criteria:
- Acute renal failure.
- Pregnant or lactating women.
- Active infection duration.
- One of infectious serum markers of HIV, syphilis, hepatitis B and hepatitis C is positive.
- Any other conditions that the investigator considers impossible to join this trial.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Technical survival rate
Time Frame: 8 year
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Technical survival of peritoneal dialysis
|
8 year
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
D/P
Time Frame: 1,2,3,4,5,6,7,8 year
|
Ratio of substance content in peritoneal dialysate to that in blood.
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1,2,3,4,5,6,7,8 year
|
|
Ccr
Time Frame: 1,2,3,4,5,6,7,8 year
|
Creatinine clearance rate.
Ccr=urinary creatinine concentration * urine volume per minute/blood creatinine concentration.
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1,2,3,4,5,6,7,8 year
|
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Kt/V
Time Frame: 1,2,3,4,5,6,7,8 year
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Ratio of urea clearance to volume during unit dialysis time.
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1,2,3,4,5,6,7,8 year
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Cell counting
Time Frame: 1,2,3,4,5,6,7,8 year
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Count the number of cells.
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1,2,3,4,5,6,7,8 year
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Electrolyte
Time Frame: 1,2,3,4,5,6,7,8 year
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Content of ions.
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1,2,3,4,5,6,7,8 year
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Blood biochemical index
Time Frame: 1,2,3,4,5,6,7,8 year
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Venous blood was obtained for biochemical examination.
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1,2,3,4,5,6,7,8 year
|
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Urine protein
Time Frame: 1,2,3,4,5,6,7,8 year
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Urine test for protein content.
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1,2,3,4,5,6,7,8 year
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Histopathology
Time Frame: 1,2,3,4,5,6,7,8 year
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With the consent of the patients, peritoneal tissue was taken to observe histological changes.
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1,2,3,4,5,6,7,8 year
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OCG
Time Frame: 1,2,3,4,5,6,7,8 year
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Glucose transport rates measured by a double mini peritoneal equilibration test.
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1,2,3,4,5,6,7,8 year
|
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Single-cell transcriptome sequencing
Time Frame: 1,2,3,4,5,6,7,8 year
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With the consent of the patients, tissues were taken for analysis.
Isolate cells in the tissues and measure gene expression profiles.
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1,2,3,4,5,6,7,8 year
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- S2021-263-01
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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